803-67-8

Basic information

• Product Name: (2Z)-5-benzylidene-3-phenyl-2-(phenylimino)-1,3-thiazolidin-4-one
• CAS NO: 803-67-8
• Molecular Formula: C₂₂H₁₆N₂OS
• Molecular Weight: 356.4402
• Mol File: 803-67-8.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 519.7°C at 760 mmHg
• Flash Point: 268.1°C
• Density: 1.18g/cm³
• Vapor Pressure: 6.65E-11mmHg at 25°C
• Refractive Index: 1.65
• CAS DataBase Reference: (2Z)-5-benzylidene-3-phenyl-2-(phenylimino)-1,3-thiazolidin-4-one(CAS DataBase Reference)
• NIST Chemistry Reference: (2Z)-5-benzylidene-3-phenyl-2-(phenylimino)-1,3-thiazolidin-4-one(803-67-8)
• EPA Substance Registry System: (2Z)-5-benzylidene-3-phenyl-2-(phenylimino)-1,3-thiazolidin-4-one(803-67-8)

Safety Data

• Hazardous Substances Data: 803-67-8(Hazardous Substances Data)

Usage

General Description

The chemical "(2Z)-5-benzylidene-3-phenyl-2-(phenylimino)-1,3-thiazolidin-4-one" is a compound that belongs to the thiazolidin-4-one class of compounds. It contains a thiazolidin-4-one ring with a benzylidene and phenylimino substituent. (2Z)-5-benzylidene-3-phenyl-2-(phenylimino)-1,3-thiazolidin-4-one has potential biological and pharmacological activities, including anti-inflammatory, anti-cancer, anti-bacterial, and anti-fungal properties. It is also used as a starting material in organic synthesis for the preparation of various pharmaceutical agents and biologically active compounds. The structural and chemical properties of this compound make it a versatile and important molecule in medicinal and pharmaceutical research.

Upstream product

• 102-08-9 N,N-diphenylthiourea 
• 7299-58-3 phenylpropiolyl chloride 
• 790-04-5 3-phenyl-2-(phenylimino)-1,3-thiazolidin-4-one 
• 100-52-7 benzaldehyde 

Downstream Products

• 1262233-76-0 1-[3,7-diphenyl-2-(phenylimino)-2,3-dihydro[1,3]thiazolo[4,5-d]pyrimidin-5-yl]thiourea 
• 1262233-81-7 2-{[3,7-diphenyl-2-(phenylimino)-2,3-dihydro[1,3]thiazolo[4,5-d]pyrimidin-5-yl]imino}-1,3-thiazolidin-4-one 
• 1262233-86-2 2-{[3,7-diphenyl-2-(phenylimino)-2,3-dihydro[1,3]thiazolo[4,5-d]pyrimidin-5-yl]imino}-3-ethoxyphthalimido-1,3-thiazolidin-4-one 
• 1262233-71-5 3,7-diphenyl-2-(phenylimino)-2,3-dihydro[1,3]thiazolo[4,5-d]pyrimidin-5-amine 
• 137513-68-9 Phenyl-[2,3,6-triphenyl-2,6-dihydro-pyrazolo[3,4-d]thiazol-(5Z)-ylidene]-amine 
• 42518-27-4 5-Benzyliden-3-phenylthiazolidin-2,4-dion 
• 2622-60-8 1-phenyl-1H-benzoimidazole 
• 103-72-0 phenyl isothiocyanate 
• 62-53-3 aniline 
• 102-08-9 N,N-diphenylthiourea 
• 102-07-8 bis(diphenyl)urea 
• 95-15-8 Benzo[b]thiophene 
• 137537-00-9 [3,6-Diphenyl-2,3,3a,6-tetrahydro-pyrazolo[3,4-d]thiazol-(5Z)-ylidene]-phenyl-amine 
• 137513-66-7 [2-(4-Nitro-phenyl)-3,6-diphenyl-2,3,3a,6-tetrahydro-pyrazolo[3,4-d]thiazol-(5Z)-ylidene]-phenyl-amine 

Relevant articles and documents

Synthesis, crystal structure and biological evaluation of 5-arylidine derivatives of 3-phenyl-2-(phenylimino)thiazolidin-4-one

Summary: Arylidene derivatives of 3-phenyl-2-(phenylimino)thiazolidin-4-ones are prepared by its condensation with respective aromatic aldehydes. The structures of synthesized compounds are established using FTIR, 13C-NMR, 1H-NMR, mass spectrometry. The s

Introduction of selenium to heterocyclic compounds. Part VI. Synthesis of 3-aryl-5-benzylidene- and 3-aryl-5-cinnamylidene-2-selenorhodanines

Three new 3-aryl-5-benzylidene-2-selenorhodanines and seven new 3-aryl-5-cinnamylidene-2-selenorhodanines were obtained by treatment with H2Se of methylation products of appropriate 2-iminothiazolidine-4-one derivatives.